These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

196 related items for PubMed ID: 960411

  • 21. [Chronic hereditary nephropathy with deafness and ocular lesions].
    Hauser J.
    Schweiz Med Wochenschr; 1974 May 18; 104(20):724-8. PubMed ID: 4829630
    [No Abstract] [Full Text] [Related]

  • 22. [Contribution to the study of Alport's syndrome. Apropos of a case].
    Schneegans E, Rohmer A, Levy-Silagy J, el-Mejjati A, Sengel A, Stoebner P, Laforgue D.
    Ann Pediatr (Paris); 1971 Dec 14; 18(12):757-69. PubMed ID: 5004890
    [No Abstract] [Full Text] [Related]

  • 23. [Alport's syndrome. Case reports].
    Varese LA, Antioniola P, Barbero S.
    Minerva Pediatr; 1978 Nov 30; 30(22):1843-52. PubMed ID: 723832
    [No Abstract] [Full Text] [Related]

  • 24. Autosomal dominant Alport's syndrome: study of a large Tunisian family.
    Kharrat M, Makni S, Makni K, Kammoun K, Charfeddine K, Azaeiz H, Jarraya F, Ben Hmida M, Gubler MC, Ayadi H, Hachicha J.
    Saudi J Kidney Dis Transpl; 2006 Sep 30; 17(3):320-5. PubMed ID: 16970251
    [Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29. [Alport's syndrome].
    Knotková V, Stejskal J, Voldrich L, Beran M, Straková M, Tomásek R.
    Sb Lek; 1973 Jun 30; 75(6):169-76. PubMed ID: 4709456
    [No Abstract] [Full Text] [Related]

  • 30. Ocular signs in Alport's syndrome.
    Thompson SM, Deady JP, Willshaw HE, White RH.
    Eye (Lond); 1987 Jun 30; 1 ( Pt 1)():146-53. PubMed ID: 3556654
    [Abstract] [Full Text] [Related]

  • 31. [Alport's syndrome with familial abnormality of the external ear].
    Firek H.
    Przegl Lek; 1984 Jun 30; 41(10):633-5. PubMed ID: 6545706
    [No Abstract] [Full Text] [Related]

  • 32. [Alport's Syndrome. Hereditary nephritis, perceptive deafness and lens anomalies].
    Norrelund N.
    Ugeskr Laeger; 1971 Mar 19; 133(11):503-5. PubMed ID: 5092560
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34. [New findings on hereditary chronic nephritis (Alport's syndrome)].
    Sarre H, Rother K, Schmitt C, Unger HH, Beickert P, Baitsch H.
    Arch Klin Med; 1966 Mar 19; 212(1):1-30. PubMed ID: 5967085
    [No Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36. Familial hereditary nephropathy (Alport's syndrome).
    Purriel P, Drets M, Pascale E, Sánchez Cestau R, Borrás A, Ferreira WA, de Lucca A, Fernández L.
    Am J Med; 1970 Dec 19; 49(6):753-73. PubMed ID: 5006614
    [No Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39. Lenticonus in Alport's syndrome. A family study.
    Singh DS, Bisht DB, Kapoor S, Sharma RN, Sankaran K, Majumdar NK.
    Acta Ophthalmol (Copenh); 1977 Feb 19; 55(1):164-9. PubMed ID: 576544
    [Abstract] [Full Text] [Related]

  • 40. A Sri Lankan family with Alport's syndrome.
    Angunawela P, Mahamiththawa U.
    Ceylon Med J; 1998 Mar 19; 43(1):56-7. PubMed ID: 9624855
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 10.